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Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Repository for lectin-assisted multimodality data
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Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▼ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0090128 | Carvajal syndrome | HGNC:3052 | Homo sapiens (human) | 1832 | DSP |
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| DOID:2219 | Glanzmann's thrombasthenia | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:10584 | retinitis pigmentosa | HGNC:2151 | Homo sapiens (human) | 1258 | CNGB1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0050657 | Bannayan-Riley-Ruvalcaba syndrome | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0050886 | Troyer syndrome | HGNC:18514 | Homo sapiens (human) | 23111 | SPART |
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| DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:1067 | open-angle glaucoma | HGNC:7610 | Homo sapiens (human) | 4653 | MYOC |
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| DOID:0112068 | nuclear type mitochondrial complex I deficiency 5 | HGNC:7707 | Homo sapiens (human) | 4719 | NDUFS1 |
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| DOID:0110142 | Bartter disease type 1 | HGNC:10910 | Homo sapiens (human) | 6557 | SLC12A1 |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | HGNC:27337 | Homo sapiens (human) | 203859 | ANO5 |
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| DOID:0081326 | oxoglutarate dehydrogenase deficiency | HGNC:8124 | Homo sapiens (human) | 4967 | OGDH |
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| DOID:0110033 | autosomal recessive Alport syndrome | HGNC:2206 | Homo sapiens (human) | 1286 | COL4A4 |
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| DOID:0060861 | microphthalmia with limb anomalies | HGNC:20318 | Homo sapiens (human) | 64093 | SMOC1 |
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| DOID:0110552 | autosomal dominant nonsyndromic deafness 22 | HGNC:7605 | Homo sapiens (human) | 4646 | MYO6 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:10768 | Homo sapiens (human) | 23451 | SF3B1 |
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| DOID:10763 | hypertension | HGNC:5141 | Homo sapiens (human) | 3240 | HP |
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| DOID:0080051 | acromesomelic dysplasia, Hunter-Thompson type | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | HGNC:8516 | Homo sapiens (human) | 340990 | OTOG |
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| DOID:0050661 | vitelliform macular dystrophy | HGNC:18362 | Homo sapiens (human) | 50939 | IMPG2 |
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| DOID:9351 | diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5006 | Homo sapiens (human) | 3156 | HMGCR |
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| DOID:10763 | hypertension | HGNC:7873 | Homo sapiens (human) | 4843 | NOS2 |
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| DOID:5844 | myocardial infarction | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:2842 | Jervell-Lange Nielsen syndrome | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
|
